ClinVar Miner

List of variants in gene combination LOC126860438, NBN reported as benign for neoplasm of immature B and T cells

Included ClinVar conditions (13):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002485.5(NBN):c.1914+9C>T	rs13312938	0.01874
NM_002485.5(NBN):c.1882G>A (p.Glu628Lys)	rs115321485	0.00466

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